US20090062357A1

US20090062357A1 - Deuterium-enriched fluconazole

Info

Publication number: US20090062357A1
Application number: US12/195,956
Authority: US
Inventors: Anthony W. Czarnik
Original assignee: Protia LLC
Current assignee: Protia LLC
Priority date: 2007-08-29
Filing date: 2008-08-21
Publication date: 2009-03-05

Abstract

The present application describes deuterium-enriched fluconazole, pharmaceutically acceptable salt forms thereof, and methods of treating using the same.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application claims priority benefit under 35 U.S.C. §119(e) of U.S. Provisional Patent Application Ser. No. 60/968,597 filed 29 Aug. 2007. The disclosure of this application is incorporated herein by reference.

FIELD OF THE INVENTION

This invention relates generally to deuterium-enriched fluconazole, pharmaceutical compositions containing the same, and methods of using the same.

BACKGROUND OF THE INVENTION

Fluconazole, shown below, is a well known triazole antifungal drug.
Since fluconazole is a known and useful pharmaceutical, it is desirable to discover novel derivatives thereof. Fluconazole is described in U.S. Pat. No. 4,404,216; the contents of which are incorporated herein by reference.

SUMMARY OF THE INVENTION

Accordingly, one object of the present invention is to provide deuterium-enriched fluconazole or a pharmaceutically acceptable salt thereof.
It is another object of the present invention to provide pharmaceutical compositions comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of at least one of the deuterium-enriched compounds of the present invention or a pharmaceutically acceptable salt thereof.
It is another object of the present invention to provide a method for treating superficial and systemic fungal infections, comprising administering to a host in need of such treatment a therapeutically effective amount of at least one of the deuterium-enriched compounds of the present invention or a pharmaceutically acceptable salt thereof.
It is another object of the present invention to provide a novel deuterium-enriched fluconazole or a pharmaceutically acceptable salt thereof for use in therapy.
It is another object of the present invention to provide the use of a novel deuterium-enriched fluconazole or a pharmaceutically acceptable salt thereof for the manufacture of a medicament (e.g., for the treatment of superficial and systemic fungal infections).
These and other objects, which will become apparent during the following detailed description, have been achieved by the inventor's discovery of the presently claimed deuterium-enriched fluconazole.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

Deuterium (D or ²H) is a stable, non-radioactive isotope of hydrogen and has an atomic weight of 2.0144. Hydrogen naturally occurs as a mixture of the isotopes ¹H (hydrogen or protium), D (²H or deuterium), and T (³H or tritium). The natural abundance of deuterium is O.015%. One of ordinary skill in the art recognizes that in all chemical compounds with a H atom, the H atom actually represents a mixture of H and D, with about 0.015% being D. Thus, compounds with a level of deuterium that has been enriched to be greater than its natural abundance of 0.015%, should be considered unnatural and, as a result, novel over their non-enriched counterparts.
All percentages given for the amount of deuterium present are mole percentages.
It can be quite difficult in the laboratory to achieve 100% deuteration at any one site of a lab scale amount of compound (e.g., milligram or greater). When 100% deuteration is recited or a deuterium atom is specifically shown in a structure, it is assumed that a small percentage of hydrogen may still be present. Deuterium-enriched can be achieved by either exchanging protons with deuterium or by synthesizing the molecule with enriched starting materials.
The present invention provides deuterium-enriched fluconazole or a pharmaceutically acceptable salt thereof. There are twenty hydrogen atoms in the fluconazole portion of fluconazole as show by variables R₁-R₁₂in formula I below.
The hydrogens present on fluconazole have different capacities for exchange with deuterium. Hydrogen atom R₁is easily exchangeable under physiological conditions and, if replaced by a deuterium atom, it is expected that it will readily exchange for a proton after administration to a patient. The remaining hydrogen atoms are not easily exchangeable and may be incorporated by the use of deuterated starting materials or intermediates during the construction of fluconazole.
The present invention is based on increasing the amount of deuterium present in fluconazole above its natural abundance. This increasing is called enrichment or deuterium-enrichment. If not specifically noted, the percentage of enrichment refers to the percentage of deuterium present in the compound, mixture of compounds, or composition. Examples of the amount of enrichment include from about 0.5, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 16, 21, 25, 29, 33, 37, 42, 46, 50, 54, 58, 63, 67, 71, 75, 79, 84, 88, 92, 96, to about 100 mol %. Since there are 12 hydrogens in fluconazole, replacement of a single hydrogen atom with deuterium would result in a molecule with about 8% deuterium enrichment. In order to achieve enrichment less than about 8%, but above the natural abundance, only partial deuteration of one site is required. Thus, less than about 8% enrichment would still refer to deuterium-enriched fluconazole.
With the natural abundance of deuterium being 0.015%, one would expect that for approximately every 6,667 molecules of fluconazole (1/0.00015=6,667), there is one naturally occurring molecule with one deuterium present. Since fluconazole has 12 positions, one would roughly expect that for approximately every 80,004 molecules of fluconazole (12×6,667), all 12 different, naturally occurring, mono-deuterated fluconazoles would be present. This approximation is a rough estimate as it doesn't take into account the different exchange rates of the hydrogen atoms on fluconazole. For naturally occurring molecules with more than one deuterium, the numbers become vastly larger. In view of this natural abundance, the present invention, in an embodiment, relates to an amount of an deuterium enriched compound, whereby the enrichment recited will be more than naturally occurring deuterated molecules.
In view of the natural abundance of deuterium-enriched fluconazole, the present invention also relates to isolated or purified deuterium-enriched fluconazole. The isolated or purified deuterium-enriched fluconazole is a group of molecules whose deuterium levels are above the naturally occurring levels (e.g., 8%). The isolated or purified deuterium-enriched fluconazole can be obtained by techniques known to those of skill in the art (e.g., see the syntheses described below).
The present invention also relates to compositions comprising deuterium-enriched fluconazole. The compositions require the presence of deuterium-enriched fluconazole which is greater than its natural abundance. For example, the compositions of the present invention can comprise (a) a μg of a deuterium-enriched fluconazole; (b) a mg of a deuterium-enriched fluconazole; and, (c) a gram of a deuterium-enriched fluconazole.
In an embodiment, the present invention provides an amount of a novel deuterium-enriched fluconazole.
Examples of amounts include, but are not limited to (a) at least 0.01, 0.02, 0.03, 0.04, 0.05, 0.1, 0.2, 0.3, 0.4, 0.5, to 1 mole, (b) at least 0.1 moles, and (c) at least 1 mole of the compound. The present amounts also cover lab-scale (e.g., gram scale), kilo-lab scale (e.g., kilogram scale), and industrial or commercial scale (e.g., multi-kilogram or above scale) quantities as these will be more useful in the actual manufacture of a pharmaceutical. Industrial/commercial scale refers to the amount of product that would be produced in a batch that was designed for clinical testing, formulation, sale/distribution to the public, etc.
In another embodiment, the present invention provides a novel, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof.
wherein R₁-R₁₂are independently selected from H and D; and the abundance of deuterium in R₁-R₁₂is at least 8%. The abundance can also be (a) at least 17%, (b) at least 25%, (c) at least 33%, (d) at least 42%, (e) at least 50%, (f) at least 58%, (g) at least 67%, (h) at least 75%, (i) at least 83%, (j) at least 92%, and (k) 100%.
In another embodiment, the present invention provides a novel, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof, wherein the abundance of deuterium in R₁is at least 100%.
In another embodiment, the present invention provides a novel, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof, wherein the abundance of deuterium in R₂-R₄is at least 33%. The abundance can also be (a) at least 67%, and (b) 100%.
In another embodiment, the present invention provides a novel, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof, wherein the abundance of deuterium in R₅-R₆is at least 50%. The abundance can also be (a) 100%.
In another embodiment, the present invention provides a novel, deuterium enriched compound of formula I, wherein the abundance of deuterium in R₅-R6 and R₁₁-R₁₂is at least 25%. The abundance can also be (a) at least 50%, (b) at least 75%, and (c) 100%.
In another embodiment, the present invention provides a novel, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof, wherein the abundance of deuterium in R₇-R₈is at least 50%. The abundance can also be (a) 100%.
In another embodiment, the present invention provides a novel, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof, wherein the abundance of deuterium in R₇-R₁₀is at least 25%. The abundance can also be (a) at least 50%, (b) at least 75%, and (c) 100%.
In another embodiment, the present invention provides an isolated novel, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof.
wherein R₁-R₁₂are independently selected from H and D; and the abundance of deuterium in R₁-R₁₂is at least 8%. The abundance can also be (a) at least 17%, (b) at least 25%, (c) at least 33%, (d) at least 42%, (e) at least 50%, (f) at least 58%, (g) at least 67%, (h) at least 75%, (i) at least 83%, (j) at least 92%, and (k) 100%.
In another embodiment, the present invention provides an isolated novel, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof, wherein the abundance of deuterium in R₁is at least 100%.
In another embodiment, the present invention provides an isolated novel, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof, wherein the abundance of deuterium in R₂-R₄is at least 33%. The abundance can also be (a) at least 67%, and (b) 100%.
In another embodiment, the present invention provides an isolated novel, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof, wherein the abundance of deuterium in R₅-R6 is at least 50%. The abundance can also be (a) 100%.
In another embodiment, the present invention provides an isolated novel, deuterium enriched compound of formula I, wherein the abundance of deuterium in R₅-R₆and R₁-R₁₂is at least 25%. The abundance can also be (a) at least 50%, (b) at least 75%, and (c) 100%.
In another embodiment, the present invention provides an isolated novel, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof, wherein the abundance of deuterium in R₇-R₈is at least 50%. The abundance can also be (a) 100%.
In another embodiment, the present invention provides an isolated novel, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof, wherein the abundance of deuterium in R₇-R₁₀is at least 25%. The abundance can also be (a) at least 50%, (b) at least 75%, and (c) 100%.
In another embodiment, the present invention provides novel mixture of deuterium enriched compounds of formula I or a pharmaceutically acceptable salt thereof.
wherein R₁-R₁₂are independently selected from H and D; and the abundance of deuterium in R₁-R₁₂is at least 8%. The abundance can also be (a) at least 17%, (b) at least 25%, (c) at least 33%, (d) at least 42%, (e) at least 50%, (f) at least 58%, (g) at least 67%, (h) at least 75%, (i) at least 83%, (j) at least 92%, and (k) 100%.
In another embodiment, the present invention provides a novel mixture of, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof, wherein the abundance of deuterium in R₁is at least 100%.
In another embodiment, the present invention provides a novel mixture of, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof, wherein the abundance of deuterium in R₂-R₄is at least 33%. The abundance can also be (a) at least 67%, and (b) 100%.
In another embodiment, the present invention provides a novel mixture of, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof, wherein the abundance of deuterium in R₅-R6 is at least 50%. The abundance can also be (a) 100%.
In another embodiment, the present invention provides a novel mixture of, deuterium enriched compound of formula I, wherein the abundance of deuterium in R₅-R₆and R₁-R₁₂is at least 25%. The abundance can also be (a) at least 50%, (b) at least 75%, and (c) 100%.
In another embodiment, the present invention provides a novel mixture of, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof, wherein the abundance of deuterium in R₇-R₈is at least 50%. The abundance can also be (a) 100%.
In another embodiment, the present invention provides a novel mixture of, deuterium enriched compound of formula I or a pharmaceutically acceptable salt thereof, wherein the abundance of deuterium in R₇-R₁₀is at least 25%. The abundance can also be (a) at least 50%, (b) at least 75%, and (c) 100%.
In another embodiment, the present invention provides novel pharmaceutical compositions, comprising: a pharmaceutically acceptable carrier and a therapeutically effective amount of a deuterium-enriched compound of the present invention.
In another embodiment, the present invention provides a novel method for treating superficial and systemic fungal infections comprising: administering to a patient in need thereof a therapeutically effective amount of a deuterium-enriched compound of the present invention.
In another embodiment, the present invention provides an amount of a deuterium-enriched compound of the present invention as described above for use in therapy.
In another embodiment, the present invention provides the use of an amount of a deuterium-enriched compound of the present invention for the manufacture of a medicament (e.g., for the treatment of superficial and systemic fungal infections).
The present invention may be embodied in other specific forms without departing from the spirit or essential attributes thereof. This invention encompasses all combinations of preferred aspects of the invention noted herein. It is understood that any and all embodiments of the present invention may be taken in conjunction with any other embodiment or embodiments to describe additional more preferred embodiments. It is also to be understood that each individual element of the preferred embodiments is intended to be taken individually as its own independent preferred embodiment. Furthermore, any element of an embodiment is meant to be combined with any and all other elements from any embodiment to describe an additional embodiment.

Definitions

The examples provided in the definitions present in this application are non-inclusive unless otherwise stated. They include but are not limited to the recited examples.
The compounds of the present invention may have asymmetric centers. Compounds of the present invention containing an asymmetrically substituted atom may be isolated in optically active or racemic forms. It is well known in the art how to prepare optically active forms, such as by resolution of racemic forms or by synthesis from optically active starting materials. All processes used to prepare compounds of the present invention and intermediates made therein are considered to be part of the present invention. All tautomers of shown or described compounds are also considered to be part of the present invention.
“Host” preferably refers to a human. It also includes other mammals including the equine, porcine, bovine, feline, and canine families.
“Treating” or “treatment” covers the treatment of a disease-state in a mammal, and includes: (a) preventing the disease-state from occurring in a mammal, in particular, when such mammal is predisposed to the disease-state but has not yet been diagnosed as having it; (b) inhibiting the disease-state, e.g., arresting it development; and/or (c) relieving the disease-state, e.g., causing regression of the disease state until a desired endpoint is reached. Treating also includes the amelioration of a symptom of a disease (e.g., lessen the pain or discomfort), wherein such amelioration may or may not be directly affecting the disease (e.g., cause, transmission, expression, etc.).
“Therapeutically effective amount” includes an amount of a compound of the present invention that is effective when administered alone or in combination to treat the desired condition or disorder. “Therapeutically effective amount” includes an amount of the combination of compounds claimed that is effective to treat the desired condition or disorder. The combination of compounds is preferably a synergistic combination. Synergy, as described, for example, by Chou and Talalay, Adv. Enzyme Regul. 1984, 22:27-55, occurs when the effect of the compounds when administered in combination is greater than the additive effect of the compounds when administered alone as a single agent. In general, a synergistic effect is most clearly demonstrated at sub-optimal concentrations of the compounds. Synergy can be in terms of lower cytotoxicity, increased antiviral effect, or some other beneficial effect of the combination compared with the individual components.
“Pharmaceutically acceptable salts” refer to derivatives of the disclosed compounds wherein the parent compound is modified by making acid or base salts thereof. Examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of the basic residues. The pharmaceutically acceptable salts include the conventional quaternary ammonium salts of the parent compound formed, for example, from non-toxic inorganic or organic acids. For example, such conventional non-toxic salts include, but are not limited to, those derived from inorganic and organic acids selected from 1,2-ethanedisulfonic, 2-acetoxybenzoic, 2-hydroxyethanesulfonic, acetic, ascorbic, benzenesulfonic, benzoic, bicarbonic, carbonic, citric, edetic, ethane disulfonic, ethane sulfonic, fumaric, glucoheptonic, gluconic, glutamic, glycolic, glycollyarsanilic, hexylresorcinic, hydrabamic, hydrobromic, hydrochloric, hydroiodide, hydroxymaleic, hydroxynaphthoic, isethionic, lactic, lactobionic, lauryl sulfonic, maleic, malic, mandelic, methanesulfonic, napsylic, nitric, oxalic, pamoic, pantothenic, phenylacetic, phosphoric, polygalacturonic, propionic, salicyclic, stearic, subacetic, succinic, sulfamic, sulfanilic, sulfuric, tannic, tartaric, and toluenesulfonic.

Synthesis

Scheme 1 shows a route to fluconazole (Richardson, U.S. Pat. No. 4,404,216).
Scheme 2 shows how various deuterated starting materials and intermediates from Scheme 1 can be accessed and used to make deuterated fluconazole analogs. A person skilled in the art of organic synthesis will recognize that these reactions and these materials may be used in various combinations to access a variety of deuterated fluconazoles. The use of known deuterated 1,3-difluorobenzenes 1-3 (Scheme 2) in place of 1,3-difluorobenzene in Scheme 1 affords deuterated fluconazoles. The use of 1 in the chemistry of Scheme 1 gives fluconazole with R₂=D. The use of 2 in the chemistry of Scheme 1 gives fluconazole with R₂-R₃=D. The use of 3 in the chemistry of Scheme 1 gives fluconazole with R₃=D. The use of commercially available trideuterio 1,2,4-triazole 4 as shown in equation (1) affords 5, which when used in the chemistry of Scheme 1 gives fluconazole with R₅-R₆=D (or R₁₁-R₁₂=D) as a racemic mixture. Compound 6 can be made as shown in equation (2) by exchange of weakly acidic hydrogen atoms next to a carbonyl group. The use of 6 in the chemistry of Scheme 1 gives fluconazole with R₇-R₈=D (or R₉-R₁₀=D) as a racemic mixture. The use of a deuterated sulfoxonium ylide as shown in equation (3) gives 7, which when used in the chemistry of Scheme 1 gives fluconazole with R₇-R₈=D (or R₉-R₁₀=D) as a racemic mixture. The use of commercially available trideuterio 1,2,4-triazole 4 as shown in equation (4) affords 8, which when used in the chemistry of Scheme 1 gives fluconazole with R₅-R₆=D (or R₁₁-R₁₂=D) as a racemic mixture.
A person skilled in the art of organic synthesis will recognize that combinations of these processes will afford even more deuterated analogs of fluconazole. For example, using the chemistry from equation (1) with that of equation (4) produces fluconazole with R₅, R₆, R₁₁, and R₁₂=D. Notably, this compound is achiral, avoiding the racemic mixture afforded if only equation (1) or equation (4) is used. A similar situation applies to the use of equations (2) and (3) together: An achiral compound results (R₇-R₁₀=D), rather than a racemic mixture if only equation (2) or equation (3) is used.

EXAMPLES

Table 1 provides compounds that are representative examples of the present invention. When one of R₁-R₂₅is present, it is selected from H or D.


	1

	2

	3

	4

	5

	6

	7

Table 2 provides compounds that are representative examples of the present invention. Where H is shown, it represents naturally abundant hydrogen.


	8

	9

	10

	11

	12

	13

	14

Numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that within the scope of the appended claims, the invention may be practiced otherwise that as specifically described herein.

Claims

1. A deuterium-enriched compound of formula I or a pharmaceutically acceptable salt thereof:

wherein R₁-R₁₂are independently selected from H and D; and

the abundance of deuterium in R₁-R₁₂is at least 8%.

2. A deuterium-enriched compound of claim 1, wherein the abundance of deuterium in R₁-R₁₂is selected from at least 8%, at least 17%, at least 25%, at least 33%, at least 42%, at least 50%, at least 58%, at least 67%, at least 75%, at least 83%, at least 92%, and 100%.

3. A deuterium-enriched compound of claim 1, wherein the abundance of deuterium in R₁is selected from at least 100%.

4. A deuterium-enriched compound of claim 1, wherein the abundance of deuterium in R₂-R₄is selected from at least 33%, at least 67%, and 100%.

5. A deuterium-enriched compound of claim 1, wherein the abundance of deuterium in R₅-R₆is selected from at least 50%, and 100%.

6. A deuterium-enriched compound of claim 1, wherein the abundance of deuterium in R₅-R₆and R₁₁-R₁₂is selected from at least 25%, at least 50%, at least 75%, and 100%.

7. A deuterium-enriched compound of claim 1, wherein the abundance of deuterium in R₇-R₈is selected from at least 50%, and 100%.

8. A deuterium-enriched compound of claim 1, wherein the abundance of deuterium in R₇-R₁O is selected from at least 25%, at least 50%, at least 75%, and 100%.

9. A deuterium-enriched compound of claim 1, wherein the compound is selected from compounds 1-7 of Table 1.

10. A deuterium-enriched compound of claim 1, wherein the compound is selected from compounds 8-14 of Table 2.

11. An isolated deuterium-enriched compound of formula I or a pharmaceutically acceptable salt thereof:

wherein R₁-R₁₂are independently selected from H and D; and

the abundance of deuterium in R₁-R₁₂is at least 8%.

12. An isolated deuterium-enriched compound of claim 11, wherein the abundance of deuterium in R₁-R₁₂is selected from at least 8%, at least 17%, at least 25%, at least 33%, at least 42%, at least 50%, at least 58%, at least 67%, at least 75%, at least 83%, at least 92%, and 100%.

13. An isolated deuterium-enriched compound of claim 11, wherein the abundance of deuterium in R₁is selected from at least 100%.

14. An isolated deuterium-enriched compound of claim 11, wherein the compound is selected from compounds 1-7 of Table 1.

15. An isolated deuterium-enriched compound of claim 11, wherein the compound is selected from compounds 8-14 of Table 2.

16. A mixture of deuterium-enriched compounds of formula I or a pharmaceutically acceptable salt thereof:

wherein R₁-R₁₂are independently selected from H and D; and

the abundance of deuterium in R₁-R₁₂is at least 8%.

17. A mixture of deuterium-enriched compounds of claim 16, wherein the compounds are selected from compounds 1-7 of Table 1.

18. A mixture of deuterium-enriched compounds of claim 16, wherein the compounds are selected from compounds 8-14 of Table 2.

19. A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of claim 1 or a pharmaceutically acceptable salt form thereof.

20. A method for treating superficial and systemic fungal infections comprising:

administering, to a patient in need thereof, a therapeutically effective amount of a compound of claim 1 or a pharmaceutically acceptable salt form thereof.